Cydonia oblonga Mill.叶乙醇提取物对离体大鼠胸主动脉的血管舒张作用及潜在作用机制叶对离体大鼠胸主动脉的作用及潜在作用机制

IF 1.5 4区 医学 Q4 CHEMISTRY, MEDICINAL Natural Product Communications Pub Date : 2024-09-07 DOI:10.1177/1934578x241282441
Donjeta Krasniqi, Albina Uka, Era Rexhbeqaj, Giangiacomo Beretta, Jasmina Petreska Stanoeva, Bujar Qazimi, Armond Daci
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引用次数: 0

摘要

目的:楙叶乙醇提取物(CydOL-EE)具有不同的心脏保护作用。然而,以前没有研究调查过它对血管平滑肌张力的直接影响。因此,本研究旨在测试 CydOL-EE 在体外大鼠胸主动脉制备中的潜在血管扩张活性,并对其作用机制进行进一步研究。研究方法首先通过 HPLC-DAD-ESI-MS/MS 对 CydOL-EE 植物化学成分进行研究,然后测试其在大鼠主动脉环中的血管舒张/血管活性效应。采用 NO 合酶抑制剂 N(ω)-硝基-L-精氨酸甲酯(L-NAME)和环鸟苷单磷酸抑制剂 1H-[1,2,4]噁二唑并[4,3-a]喹喔啉-1-酮(ODQ)来探讨 NO 依赖性途径的参与。结果CydOL-EE 的色谱分析显示,其中含有六种黄酮醇和七种羟基肉桂酸。此外,CydOL-EE 还能降低剂量依赖性苯肾上腺素(PE)引起的血管收缩活性(对照组,Emax = 104.29 ± 3.67 vs CydOL-EE,Emax = 70.73 ± 3.67,P < .0001),并能直接松弛 PE 的预收缩活性(Emax = 79.63 ± 3.67%)。这些反应在抑制 e-NOS 时消失,表明其作用机制主要受内皮依赖系统的控制。结论我们的研究结果表明,CydO-EE 可通过 NO 依赖性途径起到舒张血管和降低血管活性的作用。这些发现为进一步了解 CydOL-EE 在心血管疾病治疗中的应用提供了科学依据。
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Vasorelaxant Effects of Ethanolic Extract from Cydonia oblonga Mill. Leaves on Isolated Rat Thoracic Aorta and Potential Mechanism of Action
Objective: Cydonia oblonga Mill . leaves ethanolic extract (CydOL-EE) has shown different cardioprotective effects. However, no previous studies investigated its direct effect on the vascular smooth muscle tone. Therefore, the study aimed to test the potential vasodilator activity of CydOL-EE in ex-vivo rat thoracic aorta preparations with an additional investigation of its mechanistic effects. Methods: CydOL-EE phytochemical profile was first investigated by HPLC-DAD-ESI-MS/MS and then tested for the vasorelaxation/vasoreactivity effects in rat aortic rings. The NO synthase inhibitor N(ω)-nitro-L-arginine methyl ester (L-NAME) and cyclic guanosine monophosphate inhibitor 1H-[1,2,4]Oxadiazolo[4,3-a]quinoxalin-1-one (ODQ) were used to explore of the involvement of NO-dependent pathways. Results: Chromatographic analysis of CydOL-EE revealed the presence of six flavonols and seven hydroxycinnamic acids. Moreover, CydOL-EE showed a decrease in vasoreactivity caused by dose-dependent phenylephrine (PE) (Control, Emax = 104.29 ± 3.67 vs CydOL-EE, Emax = 70.73 ± 3.67, P < .0001) and a direct relaxing activity to precontraction with PE (Emax = 79.63 ± 3.67%). These responses were abolished during e-NOS inhibition, demonstrating that the mechanism of action was predominately controlled by the participation of an endothelium-dependent system. Conclusion: The results of our study show that CydO-EE demonstrates vasorelaxation and reduction of vasoreactivity through a NO-dependent pathway. These findings provide scientific evidence for further understanding of CydOL-EE use in the treatment of cardiovascular disease.
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来源期刊
Natural Product Communications
Natural Product Communications 工程技术-食品科技
CiteScore
3.10
自引率
11.10%
发文量
254
审稿时长
2.7 months
期刊介绍: Natural Product Communications is a peer reviewed, open access journal studying all aspects of natural products, including isolation, characterization, spectroscopic properties, biological activities, synthesis, structure-activity, biotransformation, biosynthesis, tissue culture and fermentation. It covers the full breadth of chemistry, biochemistry, biotechnology, pharmacology, and chemical ecology of natural products. Natural Product Communications is a peer reviewed, open access journal studying all aspects of natural products, including isolation, characterization, spectroscopic properties, biological activities, synthesis, structure-activity, biotransformation, biosynthesis, tissue culture and fermentation. It covers the full breadth of chemistry, biochemistry, biotechnology, pharmacology, and chemical ecology of natural products. Natural Product Communications is a peer reviewed, open access journal studying all aspects of natural products, including isolation, characterization, spectroscopic properties, biological activities, synthesis, structure-activity, biotransformation, biosynthesis, tissue culture and fermentation. It covers the full breadth of chemistry, biochemistry, biotechnology, pharmacology, and chemical ecology of natural products.
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